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Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair

The efficient transport of biological therapeutic materials to target tissues within the body is critical to their efficacy. In cartilage tissue, the lack of blood vessels prevents the entry of systemically administered drugs at therapeutic levels. Within the articulating joint complex, the dense an...

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Autores principales: Shah, Nisarg J., Geiger, Brett C., Quadir, Mohiuddin A., Hyder, Nasim, Krishnan, Yamini, Grodzinsky, Alan J., Hammond, Paula T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457159/
https://www.ncbi.nlm.nih.gov/pubmed/28584879
http://dx.doi.org/10.1002/btm2.10043
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author Shah, Nisarg J.
Geiger, Brett C.
Quadir, Mohiuddin A.
Hyder, Nasim
Krishnan, Yamini
Grodzinsky, Alan J.
Hammond, Paula T.
author_facet Shah, Nisarg J.
Geiger, Brett C.
Quadir, Mohiuddin A.
Hyder, Nasim
Krishnan, Yamini
Grodzinsky, Alan J.
Hammond, Paula T.
author_sort Shah, Nisarg J.
collection PubMed
description The efficient transport of biological therapeutic materials to target tissues within the body is critical to their efficacy. In cartilage tissue, the lack of blood vessels prevents the entry of systemically administered drugs at therapeutic levels. Within the articulating joint complex, the dense and highly charged extracellular matrix (ECM) hinders the transport of locally administered therapeutic molecules. Consequently, cartilage injury is difficult to treat and frequently results in debilitating osteoarthritis. Here we show a generalizable approach in which the electrostatic assembly of synthetic polypeptides and a protein, insulin‐like growth factor‐1 (IGF‐1), can be used as an early interventional therapy to treat injury to the cartilage. We demonstrated that poly(glutamic acid) and poly(arginine) associated with the IGF‐1 via electrostatic interactions, forming a net charged nanoscale polyelectrolyte complex (nanoplex). We observed that the nanoplex diffused into cartilage plugs in vitro and stimulated ECM production. In vivo, we monitored the transport, retention and therapeutic efficacy of the nanoplex in an established rat model of cartilage injury. A single therapeutic dose, when administered within 48 hr of the injury, conferred protection against cartilage degradation and controlled interleukin‐1 mediated inflammation. IGF‐1 contained in the nanoplex was detected in the joint space for up to 4 weeks following administration and retained bioactivity. The results indicate the potential of this approach as an early intervention therapy following joint injury to delay or even entirely prevent the onset of osteoarthritis.
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spelling pubmed-54571592017-09-01 Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair Shah, Nisarg J. Geiger, Brett C. Quadir, Mohiuddin A. Hyder, Nasim Krishnan, Yamini Grodzinsky, Alan J. Hammond, Paula T. Bioeng Transl Med Research Reports The efficient transport of biological therapeutic materials to target tissues within the body is critical to their efficacy. In cartilage tissue, the lack of blood vessels prevents the entry of systemically administered drugs at therapeutic levels. Within the articulating joint complex, the dense and highly charged extracellular matrix (ECM) hinders the transport of locally administered therapeutic molecules. Consequently, cartilage injury is difficult to treat and frequently results in debilitating osteoarthritis. Here we show a generalizable approach in which the electrostatic assembly of synthetic polypeptides and a protein, insulin‐like growth factor‐1 (IGF‐1), can be used as an early interventional therapy to treat injury to the cartilage. We demonstrated that poly(glutamic acid) and poly(arginine) associated with the IGF‐1 via electrostatic interactions, forming a net charged nanoscale polyelectrolyte complex (nanoplex). We observed that the nanoplex diffused into cartilage plugs in vitro and stimulated ECM production. In vivo, we monitored the transport, retention and therapeutic efficacy of the nanoplex in an established rat model of cartilage injury. A single therapeutic dose, when administered within 48 hr of the injury, conferred protection against cartilage degradation and controlled interleukin‐1 mediated inflammation. IGF‐1 contained in the nanoplex was detected in the joint space for up to 4 weeks following administration and retained bioactivity. The results indicate the potential of this approach as an early intervention therapy following joint injury to delay or even entirely prevent the onset of osteoarthritis. John Wiley and Sons Inc. 2016-11-18 /pmc/articles/PMC5457159/ /pubmed/28584879 http://dx.doi.org/10.1002/btm2.10043 Text en © 2016 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Shah, Nisarg J.
Geiger, Brett C.
Quadir, Mohiuddin A.
Hyder, Nasim
Krishnan, Yamini
Grodzinsky, Alan J.
Hammond, Paula T.
Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title_full Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title_fullStr Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title_full_unstemmed Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title_short Synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
title_sort synthetic nanoscale electrostatic particles as growth factor carriers for cartilage repair
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457159/
https://www.ncbi.nlm.nih.gov/pubmed/28584879
http://dx.doi.org/10.1002/btm2.10043
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